Year: 2020
Type: article
Abstract: Computationally understanding the molecular mechanisms that give rise to cell signaling responses upon different environmental, chemical, and genetic perturbations is a long-standing challenge that requires models that fit and predict quantitative responses for new biological conditions. Overcoming this challenge depends not only on good models and detailed experimental data but also on the rigorous integration of both. We propose a quantitative framework to perturb and model generic signaling networks using multiple and diverse changing environments (hereafter "kinetic stimulations") resulting in distinct pathway activation dynamics. We demonstrate that utilizing multiple diverse kinetic stimulations better constrains model parameters and enables predictions of signaling dynamics that would be impossible using traditional dose-response or individual kinetic stimulations. To demonstrate our approach, we use experimentally identified models to predict signaling dynamics in normal, mutated, and drug-treated conditions upon multitudes of kinetic stimulations and quantify which proteins and reaction rates are most sensitive to which extracellular stimulations.
Source: iScience
Authors: Hossein Jashnsaz, Zachary R. Fox, Jason J. Hughes, Guoliang Li, Brian Munsky, Gregor Neuert
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,000
Awards: G1070450565, High-Performance Computer Cluster for Biomedical Research, G1510967449, G2163872307, G3606619490, G4656594441, G6601343345, Cybergenetic circuits to test composability of gene networks, G7110204130, G7596079831, G9000000418, G9000128600, G9000252946, Integrating Multi-Scale Imaging, Reaction-Diffusion Simulation, and Markov Model Inference to Enhance Predictive Design and Interpretation of Single-Molecule Gene Regulation Experiments
OpenAlex ID: W3085516878
